|
Class 2 Device Recall Synthes MultiVector Distractor Body, Part Number 487.931 |
 |
Date Initiated by Firm |
January 11, 2013 |
Date Posted |
March 01, 2013 |
Recall Status1 |
Terminated 3 on August 31, 2015 |
Recall Number |
Z-0903-2013 |
Recall Event ID |
64195 |
510(K)Number |
K010690
|
Product Classification |
Screw, fixation, intraosseous - Product Code DZL
|
Product |
Synthes Multi-Vector Distractor Body, Part Number 487.931.
For mandibular bone lengthening. |
Code Information |
Part number 487.831 - Lot numbers 7826459,7750064, 7667285, and 7806090. |
Recalling Firm/ Manufacturer |
Synthes USA HQ, Inc. 1302 Wrights Ln E West Chester PA 19380-3417
|
For Additional Information Contact |
customer support 610-719-5000
|
Manufacturer Reason for Recall |
It was discovered that the sheer pin on the Multi-Vector Distractor may not be made according to product specifications.
|
FDA Determined Cause 2 |
Device Design |
Action |
The firm, Synthes (USA) sent an "URGENT NOTICE: MEDICAL DEVICE RECALL" letter dated January 11, 2013 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Contact the firmat 610-719-5450 for questions regarding this notice. |
Quantity in Commerce |
2 |
Distribution |
Nationwide Distribution-including the states of CO, LA, MD, MN, NY, PA, RI, TN, TX and UT. |
Total Product Life Cycle |
TPLC Device Report
|
|
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
|
510(K) Database |
510(K)s with Product Code = DZL and Original Applicant = SYNTHES (USA)
|
|
|
|